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3-(3-硝基苯基)丙醛 | 198783-53-8

中文名称
3-(3-硝基苯基)丙醛
中文别名
间硝基苯丙醛
英文名称
3-(3-nitrophenyl)propanal
英文别名
——
3-(3-硝基苯基)丙醛化学式
CAS
198783-53-8
化学式
C9H9NO3
mdl
MFCD09028611
分子量
179.175
InChiKey
DNLNGXWQNDCKFE-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    306.7±17.0 °C(Predicted)
  • 密度:
    1.211±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.7
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.222
  • 拓扑面积:
    62.9
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2913000090

SDS

SDS:db83c6b323d23c03fa28636feeddb39c
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-(3-硝基苯基)丙醛甲醇 、 sodium cyanoborohydride 、 溶剂黄146乙酰氯 作用下, 反应 15.0h, 生成
    参考文献:
    名称:
    Anhydrolide Macrolides. 2. Synthesis and Antibacterial Activity of 2,3-Anhydro-6-O-methyl 11,12-Carbazate Erythromycin A Analogues
    摘要:
    A series of 3-descladinosyl-2,3-anhydro-6-O-methylerythromycin A 11,12-cyclic carbazate analogues was prepared and evaluated for antibacterial activity. These 2,3-anhydro macrolides were found to be potent antibacterial agents in vitro against macrolide-susceptible organisms including Staphylococcus aureus 6538P, Streptococcus pyogenes EES61, and Streptococcus pneumoniae ATCC6303. These compounds were also very active against some organisms that show macrolide resistance (S. aureus A5177, S. pyogenes PIU2584, and S. pneumoniae 5649). The compounds generally showed poor activity against organisms with constitutive MLS resistance. Selected compounds were evaluated in vivo in mouse protection studies. Although most of the compounds tested in vivo showed poor efficacy, two compounds, 38 and 57, were more active than clarithromycin against S. pneumoniae ATCC6303.
    DOI:
    10.1021/jm970548p
  • 作为产物:
    描述:
    2,2-二甲基-5-(3-硝基苄基亚基)-1,3-二恶烷-4,6-二酮 在 sodium tetrahydroborate 、 溶剂黄146苯硅烷三乙胺 作用下, 以 二氯甲烷四氢呋喃 为溶剂, 反应 3.0h, 生成 3-(3-硝基苯基)丙醛
    参考文献:
    名称:
    3,5-Disubstituted-thiazolidine-2,4-dione analogs as anticancer agents: Design, synthesis and biological characterization
    摘要:
    A series of 2,5-disubstituted-thiazolidine-2,4-dione analogs based on the newly identified lead 1, a potential anticancer agent via the inhibition of the Raf/MEK/extracellular signal regulated kinase (ERK) and phosphatidylinositol 3-kinase (PI3K)/Akt signaling cascades, were synthesized and biologically characterized. A new lead structure, 15, was identified to have improved anti-proliferative activities in U937 cells, to induce apoptosis in U937, M12 and DU145 cancer cells, and to arrest U937 cells at the S-phase. Furthermore, Western blot analysis demonstrated a correlation of the anti-proliferative activity and blockade of the Raf/MEK/ERK and PI3K/Akt signaling pathways. Collectively, these results strongly encourage further optimization of 15 as a new lead with multi-target properties to develop more potent compounds as anticancer agents. (C) 2011 Elsevier Masson SAS. All rights reserved.
    DOI:
    10.1016/j.ejmech.2011.10.031
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文献信息

  • Efficient preparation of trans-α,β-unsaturated aldehydes from saturated aldehydes by oxidative enamine catalysis
    作者:ShiLei Zhang、HeXin Xie、AiGuo Song、DeYan Wu、Jin Zhu、SiHan Zhao、Jian Li、XinHong Yu、Wei Wang
    DOI:10.1007/s11426-011-4432-6
    日期:2011.12
    mild and highly efficient amine-catalyzed, IBX-mediated oxidation of aldehydes to (E) selective α,β-unsaturated aldehydes has been achieved in good yields. The process features a new oxidation of enamines to iminium ions in a catalytic fashion.
    已以良好的产率实现了温和且高效的胺催化,IBX介导的醛氧化为(E)选择性α,β-不饱和醛的氧化。该方法的特征在于以催化方式将烯胺新氧化为亚胺离子。
  • Stereoselective organocatalytic oxidation of alcohols to enals: a homologation method to prepare polyenes
    作者:Xiaobei Chen、Yinan Zhang、Huixin Wan、Wei Wang、Shilei Zhang
    DOI:10.1039/c5cc10093c
    日期:——
    A novel organocatalytic oxidation through oxidative enamine catalysis was developed with excellent compatibility for the direct syntheses of enals from simple saturated alcohols. By using this amine-catalyzed IBX-oxidation, a wide...
    开发了一种新型的通过氧化烯胺催化的有机催化氧化方法,该方法与由简单的饱和醇直接合成烯类具有优异的相容性。通过使用这种胺催化的IBX氧化,广泛的...
  • Synthesis of tetra-pincer nickel(<scp>ii</scp>) and palladium(<scp>ii</scp>) complexes of resorcin[4]arene-octophosphinite [Res(OPR<sub>2</sub>)<sub>8</sub>] and rhodium-catalyzed regioselective hydroformylation reaction
    作者:Guddekoppa S. Ananthnag、Dipanjan Mondal、Joel T. Mague、Maravanji S. Balakrishna
    DOI:10.1039/c9dt02499a
    日期:——
    The reactions of 3 with Ni(COD)2 or Pd2(dba)3·CHCl3 in appropriate molar ratios yielded tetra-pincer complexes 5 and 6, respectively. The structures of both the complexes were established by single crystal X-ray diffraction studies. The resorcin[4]arene backbone adopts a boat structure in these complexes. Typically, the Rh-catalyzed hydroformylation of styrene prevalently delivers a branched (b) chiral
    间苯二酚戊醛的缩合反应产生间苯二酚[4]芳烃1,该邻苯二酚[4]芳烃1在室温下用N-代琥珀酰亚胺化后生成四化物衍生物2。2与二苯基膦和邻亚苯基亚磷酸的反应分别产生了八亚膦酸酯3(以下称为八膦)和八亚磷酸酯4。的反应3用Ni(COD)2或Pd 2(DBA)3 ·氯仿3在适当的摩尔比,得到四-钳形络合物5和分别为6。两种配合物的结构都是通过单晶X射线衍射研究确定的。在这些配合物中,间苯二酚[4]芳烃主链采用船形结构。通常,苯乙烯的Rh催化加氢甲酰基化通常会传递支链(b)手性醛。一个独特的间苯二酚[4]基于octaphos芳烃骨架3在苯乙烯催化加氢甲酰化使用。发现属与配体的比例为1:1(M:L)的苯乙烯加氢甲酰化具有区域选择性,产生线性(l)醛作为主要产物,在3小时内转化率为100%。当苯乙烯的邻位被甲基和取代基填充时,l:b比率出人意料地增加。p的加氢甲酰化尽管硝基硝基苯
  • [EN] 2-AMINOIMIDAZOLE-PHENYL DERIVATIVES USEFUL FOR CONTROLLING MICROBIAL GROWTH<br/>[FR] DÉRIVÉS DE 2-AMINOIMIDAZOLE-PHÉNYLE UTILES POUR LUTTER CONTRE LA CROISSANCE MICROBIENNE
    申请人:UNIV NORTH CAROLINA STATE
    公开号:WO2018169752A1
    公开(公告)日:2018-09-20
    Provided are 2-aminoimidazole-phenyl derivative compounds of Formula (I): which compounds are useful in methods of controlling microbial growth, such as by enhancing the effects of an antibiotic administered in combination with the compound. Compositions including these compounds, devices including these compounds, and methods of using the same are also provided.
    提供了公式(I)的2-氨基咪唑-苯衍生物化合物,这些化合物在控制微生物生长的方法中很有用,例如通过增强与该化合物联合给药的抗生素的效果。还提供了包括这些化合物的组合物、包括这些化合物的设备以及使用它们的方法。
  • FUNCTIONALIZED MAGNETIC NANOPARTICLE, A CATALYST, A METHOD FOR FORMING C-C BONDS
    申请人:KING FAHD UNIVERSITY OF PETROLEUM AND MINERALS
    公开号:US20180099987A1
    公开(公告)日:2018-04-12
    A functionalized magnetic nanoparticle including an organometallic sandwich compound and a magnetic metal oxide. The functionalized magnetic nanoparticle may be reacted with a metal precursor to form a catalyst for various C—C bond forming reactions. The catalyst may be recovered with ease by attracting the catalyst with a magnet.
    一种功能化的磁性纳米颗粒,包括一个有机属夹层化合物和一个磁性金属氧化物。这种功能化的磁性纳米颗粒可以与属前体反应,形成用于各种C—C键形成反应的催化剂。通过用磁吸引催化剂,可以轻松回收催化剂。
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同类化合物

(βS)-β-氨基-4-(4-羟基苯氧基)-3,5-二碘苯甲丙醇 (S,S)-邻甲苯基-DIPAMP (S)-(-)-7'-〔4(S)-(苄基)恶唑-2-基]-7-二(3,5-二-叔丁基苯基)膦基-2,2',3,3'-四氢-1,1-螺二氢茚 (S)-盐酸沙丁胺醇 (S)-3-(叔丁基)-4-(2,6-二甲氧基苯基)-2,3-二氢苯并[d][1,3]氧磷杂环戊二烯 (S)-2,2'-双[双(3,5-三氟甲基苯基)膦基]-4,4',6,6'-四甲氧基联苯 (S)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (R)富马酸托特罗定 (R)-(-)-盐酸尼古地平 (R)-(-)-4,12-双(二苯基膦基)[2.2]对环芳烷(1,5环辛二烯)铑(I)四氟硼酸盐 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[((6-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(4-叔丁基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-7-双(3,5-二叔丁基苯基)膦基7''-[(3-甲基吡啶-2-基甲基)氨基]-2,2'',3,3''-四氢-1,1''-螺双茚满 (R)-(+)-4,7-双(3,5-二-叔丁基苯基)膦基-7“-[(吡啶-2-基甲基)氨基]-2,2”,3,3'-四氢1,1'-螺二茚满 (R)-3-(叔丁基)-4-(2,6-二苯氧基苯基)-2,3-二氢苯并[d][1,3]氧杂磷杂环戊烯 (R)-2-[((二苯基膦基)甲基]吡咯烷 (R)-1-[3,5-双(三氟甲基)苯基]-3-[1-(二甲基氨基)-3-甲基丁烷-2-基]硫脲 (N-(4-甲氧基苯基)-N-甲基-3-(1-哌啶基)丙-2-烯酰胺) (5-溴-2-羟基苯基)-4-氯苯甲酮 (5-溴-2-氯苯基)(4-羟基苯基)甲酮 (5-氧代-3-苯基-2,5-二氢-1,2,3,4-oxatriazol-3-鎓) (4S,5R)-4-甲基-5-苯基-1,2,3-氧代噻唑烷-2,2-二氧化物-3-羧酸叔丁酯 (4S,4''S)-2,2''-亚环戊基双[4,5-二氢-4-(苯甲基)恶唑] (4-溴苯基)-[2-氟-4-[6-[甲基(丙-2-烯基)氨基]己氧基]苯基]甲酮 (4-丁氧基苯甲基)三苯基溴化磷 (3aR,8aR)-(-)-4,4,8,8-四(3,5-二甲基苯基)四氢-2,2-二甲基-6-苯基-1,3-二氧戊环[4,5-e]二恶唑磷 (3aR,6aS)-5-氧代六氢环戊基[c]吡咯-2(1H)-羧酸酯 (2Z)-3-[[(4-氯苯基)氨基]-2-氰基丙烯酸乙酯 (2S,3S,5S)-5-(叔丁氧基甲酰氨基)-2-(N-5-噻唑基-甲氧羰基)氨基-1,6-二苯基-3-羟基己烷 (2S,2''S,3S,3''S)-3,3''-二叔丁基-4,4''-双(2,6-二甲氧基苯基)-2,2'',3,3''-四氢-2,2''-联苯并[d][1,3]氧杂磷杂戊环 (2S)-(-)-2-{[[[[3,5-双(氟代甲基)苯基]氨基]硫代甲基]氨基}-N-(二苯基甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[((1S,2S)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2S)-2-[[[[[[((1R,2R)-2-氨基环己基]氨基]硫代甲基]氨基]-N-(二苯甲基)-N,3,3-三甲基丁酰胺 (2-硝基苯基)磷酸三酰胺 (2,6-二氯苯基)乙酰氯 (2,3-二甲氧基-5-甲基苯基)硼酸 (1S,2S,3S,5S)-5-叠氮基-3-(苯基甲氧基)-2-[(苯基甲氧基)甲基]环戊醇 (1S,2S,3R,5R)-2-(苄氧基)甲基-6-氧杂双环[3.1.0]己-3-醇 (1-(4-氟苯基)环丙基)甲胺盐酸盐 (1-(3-溴苯基)环丁基)甲胺盐酸盐 (1-(2-氯苯基)环丁基)甲胺盐酸盐 (1-(2-氟苯基)环丙基)甲胺盐酸盐 (1-(2,6-二氟苯基)环丙基)甲胺盐酸盐 (-)-去甲基西布曲明 龙蒿油 龙胆酸钠 龙胆酸叔丁酯 龙胆酸 龙胆紫-d6 龙胆紫